Reply: A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation

Sylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, Emmanuelle C. Genin, Sandra Lacas-Gervais, Konstantina Fragaki, Laetitia Berg-Alonso, Yusuke Kageyama, Valérie Serre, David Moore, Annie Verschueren, Cécile Rouzier, Isabelle Le Ber, Gaëlle Augé, Charlotte Cochaud, Françoise Lespinasse, Karine N'Guyen, Anne De Septenville, Alexis Brice, Patrick Yu-Wai-ManHiromi Sesaki, Jean Pouget, Véronique Paquis-Flucklinger

Research output: Contribution to journalLetterpeer-review

Original languageEnglish (US)
Pages (from-to)e377
JournalBrain
Volume138
Issue number9
DOIs
StatePublished - Sep 1 2015

ASJC Scopus subject areas

  • Clinical Neurology

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